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British Journal of Psychiatry, 1969
The case history is reported here of a woman who has developed involuntary movements while having prolonged phenothiazine therapy. The disorder has developed gradually and is apparently irreversible. It has some unusual features.
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The case history is reported here of a woman who has developed involuntary movements while having prolonged phenothiazine therapy. The disorder has developed gradually and is apparently irreversible. It has some unusual features.
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Cytotoxic Potential of Phenothiazines
Current Drug Targets, 2006Phenothiazines, a kind of sulfur-containing tricyclic compounds, have diverse biological activities including tranquilizer, antibacterial, antitumor and antihelmintic activities due to the relatively lower cytotoxicity. Phenothiazines have been used for clinical treatments as psychotropics.
Kazue Satoh+3 more
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Cardiovascular effects of phenothiazines
American Heart Journal, 1980Abstract Phenothiazines have significant electrophysiologic and cardiocirculatory effects. The electrophysiologic effect of these drugs is similar to that reported for quinidine. Phenothiazines decrease the rate of rise of phase 0 of the action potential, decrease the duration and amplitude of phase 2, and prolong phase 3.
William Frishman+3 more
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Copper‐Catalyzed Domino Reactions for the Synthesis of Phenothiazines
, 2015A method for the one-pot synthesis of phenothiazines from benzothiazoles and aryl ortho-dihalides was explored. Preliminary work on the mechanism of the reaction suggested that it follows a domino process, including the hydrolysis of benzothiazoles ...
Manna Huang+3 more
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Paradoxical effects of phenothiazines
The Psychiatric Quarterly, 1968Four patients have been described as showing a most unusual paradoxical reaction to phenothiazines at extremely low doses. The theoretical aspects of the problem have been considered.
Herman C. B. Denber+2 more
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The Toxicity of Coroxon/Phenothiazine and Coumaphos/Phenothiazine
Research in Veterinary Science, 1962SUMMARY —Experiments are described which show that anthelmintic doses of mixtures of Coroxon/phenothiazine or Coumaphos/phenothiazine are well tolerated by sheep of all ages and by sheep under various environmental conditions. Metabolism studies with Coroxon/phenothiazine showed that over 90 per cent of an oral dose (6 mg./ kg.) of Coroxon was ...
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, 2013
A convenient method for the synthesis of various substituted phenothiazines from cyclohexanones and 2-aminobenzenethiols using molecular oxygen as hydrogen acceptor in the absence of transition-metals is described.
Yunfeng Liao+4 more
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A convenient method for the synthesis of various substituted phenothiazines from cyclohexanones and 2-aminobenzenethiols using molecular oxygen as hydrogen acceptor in the absence of transition-metals is described.
Yunfeng Liao+4 more
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Chemical Communications, 2012
A ligand-free CuI-catalyzed cascade C-S and C-N cross coupling of (hetero)aryl ortho-dihalides and ortho-aminobenzenethiols has been developed, and various phenothiazines were synthesized with excellent regioselectivity.
Chuan Dai+5 more
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A ligand-free CuI-catalyzed cascade C-S and C-N cross coupling of (hetero)aryl ortho-dihalides and ortho-aminobenzenethiols has been developed, and various phenothiazines were synthesized with excellent regioselectivity.
Chuan Dai+5 more
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Infrared Study of Phenothiazine and N-Methyl Phenothiazine
1999Phenothiazine (PhT) (fig. 1) and N-methyl phenothiazine (N-MePhT) are of special interest for their properties as photosensitizer, possible mutagen, and toxicity. Phenothiazine is employed in the preparation of carbazoles, piperazines [1] and charge-transfer semiconducting complexes [2].
J. L. Núñez+3 more
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Mechanism for Phenothiazine Oxidation
Journal of Pharmaceutical Sciences, 1977The mechanism of phenothiazine degradation was studied by following the degradation of 3,10'-diphenothiazine in ethanol-water mixtures as well as the electrochemical oxidation of phenothiazine. A mechanism, including the formation of an oxidized dimer and some polymers, is suggested.
H. Roseboom, J.H. Perrin
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